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I.E.C COLUMN

K830918 Class I Traditional
Decision Date
1983-04-27
Sponsor / Applicant
Berwick Medical Products, Inc.

Technical Specification

510(k) Submission ID K830918
Product Code KEA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2230
Decision Date 1983-04-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

I.E.C COLUMN received FDA 510(k) clearance under submission number K830918, sponsored by Berwick Medical Products, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1983-04-27.

Classification & Regulation

This clearance is catalogued under FDA product code KEA and 21 CFR 862.2230, within the Clinical Chemistry review panel as a Class I device.